Dong Ha Kim

ORCID: 0000-0002-5800-5977
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About
Contact & Profiles
Research Areas
  • Lung Cancer Treatments and Mutations
  • Synthesis and biological activity
  • HER2/EGFR in Cancer Research
  • Cancer therapeutics and mechanisms
  • Quinazolinone synthesis and applications
  • Cancer Mechanisms and Therapy
  • Pancreatic function and diabetes
  • Pancreatic and Hepatic Oncology Research
  • Phagocytosis and Immune Regulation

Hanyang University
2025

Asan Medical Center
2022-2023

University of Ulsan
2022-2023

Ulsan College
2022

Abstract Osimertinib is an irreversible third-generation EGFR tyrosine kinase inhibitor (TKI) that was initially developed to overcome the T790M mutation and used as a standard therapy in patients with advanced non–small cell lung cancer (NSCLC) EGFR-activating mutations. Despite remarkable initial efficacy, osimertinib, like other EGFR-TKIs, limited by emergence of acquired resistance. As C797S has been identified key driver resistance development drug targets this clinically relevant could...

10.1158/0008-5472.can-22-0394 article EN Cancer Research 2022-08-25

<div>Abstract<p>Osimertinib is an irreversible third-generation EGFR tyrosine kinase inhibitor (TKI) that was initially developed to overcome the T790M mutation and used as a standard therapy in patients with advanced non–small cell lung cancer (NSCLC) EGFR-activating mutations. Despite remarkable initial efficacy, osimertinib, like other EGFR-TKIs, limited by emergence of acquired resistance. As C797S has been identified key driver resistance development drug targets this...

10.1158/0008-5472.c.6514004.v1 preprint EN 2023-03-31

<div>Abstract<p>Osimertinib is an irreversible third-generation EGFR tyrosine kinase inhibitor (TKI) that was initially developed to overcome the T790M mutation and used as a standard therapy in patients with advanced non–small cell lung cancer (NSCLC) EGFR-activating mutations. Despite remarkable initial efficacy, osimertinib, like other EGFR-TKIs, limited by emergence of acquired resistance. As C797S has been identified key driver resistance development drug targets this...

10.1158/0008-5472.c.6514004 preprint EN 2023-03-31
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